NM_000039.2:c.-75=

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HGVS Expressions

  • NG_012021.1:g.4964=
  • NM_000039.2:c.-75=
  • NC_000011.10:g.116837659=

Associated Genes

Apolipoprotein A-I
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CTGA Clinical Significance

Uncertain Significance

Variant Type

Reference Allele

dbSNP

1941589418

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
145500.G.12.1United Arab Emirates120.24Uncertain SignificanceHypertension, EssentialSadaf et al. 2002 Study with 82 hypertensive patients - si...
145500.G.12.2United Arab Emirates270.24Uncertain SignificanceHypertension, EssentialSadaf et al. 2002 Study with 82 hypertensive patients - 27...
145500.G.12.3United Arab Emirates120.18Sadaf et al. 2002 Control group consisting of 80 normotens...
145500.G.12.4United Arab Emirates160.18Sadaf et al. 2002 Control group consisting of 80 normotens...
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Contributors

  • Asha Deepthi: 08.08.2022

Edit History

  • Sami Bizzari: 10.01.2023
  • Pratibha Nair: 29.11.2022
  • Asha Deepthi: 08.08.2022
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© CAGS 2024. All rights reserved.
© CAGS 2024. All rights reserved.